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. Author manuscript; available in PMC: 2009 Oct 1.
Published in final edited form as: Phytochemistry. 2008 Aug 29;69(13):2495–2500. doi: 10.1016/j.phytochem.2008.07.005

Table 2.

1H and 13C NMR spectral data of 3 (in CDCl3)

position δH (mult., J in Hz) δc DEPT position δH (mult., J in Hz) δc DEPT
1 4.38 (1H, dd, 3.5, 12) 63.4, t 10″ 2.80 (2H, m) 25.3, t
4.19 (1H, dd, 6.5, 12)
2 5.30 (1H, m) 70.5, d 11″ 5.35 (1H, m) 128.7, d
3 3.88 (1H, dd, 5.5, 11) 68.8, t 12″ 5.35 (1H, m) 128.5, d
3.73 (1H, dd, 6.5, 11)
1′ 175.0, s 13″ 2.80 (2H, m) 25.1, t
2′ 2.05 (2H, m) 34.5, t 14″ 5.35 (1H, m) 127.9, d
3′ 1.66 (2H, m) 26.0, t 15″ 5.35 (1H, m) 130.9, d
4′-14′ 1.2-1.3 (22H, m) 29.5-30.1, t 16″ 2.01 (2H, m) 27.6, t
15′ 1.34 (2H, m) 23.0, t 17″ 1.67 (2H, m) 30.6, t
16′ 0.85 (3H, t, 7) 14.5, q 18″ 1.27 (2H, m) 32.3, t
1″ 174.0, s 19″ 1.36 (2H, m) 23.1, t
2″ 2.31 (2H, m) 34.7, t 20″ 0.87 (3H, t, 7) 14.5, q
3″ 1.69 (2H, m) 33.9, t 1‴ 4.26 (1H, d, 7.5) 104.4, d
4″ 2.09 (2H, m) 26.9, t 2‴ 3.63 (1H, m) 72.1, d
5″ 5.35 (1H, m) 129.4, d 3‴ 3.99 (1H, m) 69.9, d
6″ 5.35 (1H, m) 128.2, d 4‴ 3.53 (1H, m) 74.9, d
7″ 2.80 (2H, m) 25.4, t 5‴ 3.59 (1H, m) 73.8, d
8″ 5.35 (1H, m) 129.2, d 6‴ 3.96 (1H, m) 63.2, d
3.84 (1H, m)
9″ 5.35 (1H, m) 129.0, d